Regulatory Affairs Associate

at  Carrot Pharma Recruitment

United Kingdom, , United Kingdom - 00000

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate30 Oct, 2020GBP 32000 Annual31 Jul, 20202 year(s) or aboveLatam,Medical Devices,Iso,ApacNoNo
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Description:

THE COMPANY

This is an exciting time to join an expanding, highly successful global medical devices company based at their site in Cheshire. They develop and manufacture their own products and have an excellent R&D capability ensuring they stay at the forefront of medical devices and associated technology.

  • Global, leading medical devices company
  • Manufacture and register a range of high-quality devices as well as many more in the pipeline
  • At the forefront of medical devices, particularly within wound care

Responsibilities:

THE ROLE

The Regulatory Affairs Associate will be responsible for;

  • Submit and maintain global regulatory approvals, supporting regulatory submissions for new markets and maintaining registrations and licences in existing markets.
  • Advising the business regarding any regulatory enquiries
  • Coordinate the preparation, review and submit timely responses to requests for additional information from regulatory authorities on product registrations.

To apply for this role as a Regulatory Affairs Associate our client is hoping for someone with the following skills and experience;

  • Good regulatory experience within medical devices or pharma (6 months-2 years ideally)
  • Good knowledge of MDD/MDR (desirable)
  • Good knowledge of ISO 134585
  • Ideally experienced in managing registrations in EMEA, LATAM & APAC (desirable not essential
  • Science based degre


REQUIREMENT SUMMARY

Min:2.0Max:7.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Proficient

1

United Kingdom, United Kingdom